Oral gene delivery platform based on glycol chitosan-PEG-lactoferrin conjugate
- Authors
- Jang, Seonmi; Priscilla, Lia; Lee, Chang Woo; Lee, Seung Ah; Lee, Minhyung; Lee, Dong Yun
- Issue Date
- Jan-2026
- Publisher
- ELSEVIER
- Keywords
- Gene therapy; Oral delivery; Glycol chitosan-maleimide-polyethylene glycol-N-hydroxysuccinimide ester-lactoferrin; (GPL); Fibroblast growth factor 21 (FGF21); Type 2 diabetes mellitus (T2D)
- Citation
- Journal of Controlled Release, v.389, pp 1 - 15
- Pages
- 15
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Controlled Release
- Volume
- 389
- Start Page
- 1
- End Page
- 15
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/210449
- DOI
- 10.1016/j.jconrel.2025.114463
- ISSN
- 0168-3659
1873-4995
- Abstract
- Oral gene delivery offers an alternative to parenteral administration for managing chronic metabolic disorders such as type 2 diabetes mellitus (T2D). However, its development has been limited by enzymatic degradation within the gastrointestinal tract and inefficient intestinal absorption. To overcome these obstacles, we developed a non-viral oral gene delivery system based on a glycol chitosan-maleimide-polyethylene glycol-N-hydroxysuccinimide ester-lactoferrin (GPL) platform. We then applied this platform to deliver fibroblast growth factor 21 (FGF21), a key regulator of glucose and lipid metabolism, through lactoferrin receptor–mediated transcytosis. Oral administration of the GPL/FGF21 polyplex achieved circulating FGF21 levels comparable to intraperitoneal injection. This resulted in a ∼ 37 % reduction in fasting glucose and a ∼ 47 % improvement in insulin sensitivity in high-fat diet (HFD)-induced T2D mice, accompanied by systemic FGF21 protein expression. Collectively, this GPL-based oral gene delivery system represents a promising gene therapeutic strategy with broad applicability for metabolic diseases.
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